Sodium Carbonate → HCID 90388565, compound

HRID 2205205Notes

Reaction equation

[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8](I)=[CH:9][N:10]=2)[N:7]=1.B(O)(O)[C:13]1[CH:18]=[CH:17][C:16]2[NH:19][CH:20]=[CH:21][C:15]=2[CH:14]=1.C(=O)([O-])[O-].[Na+].[Na+]>C(#N)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8]([C:13]3[CH:14]=[C:15]4[C:16](=[CH:17][CH:18]=3)[NH:19][CH:20]=[CH:21]4)=[CH:9][N:10]=2)[N:7]=1

Participants

Conditions

Temperature: 150 °C

Procedure

6-chloro-3-iodoimidazo[1,2-b]pyridazine (1.00 g, 4.30 mmol, 1.0 equiv), in acetonitrile (20 mL), was added 1H-indol-5-yl-5-boronic acid (1.04 g, 6.45 mmol, 1.5 equiv), bis(triphenylphosphine)palladium(II) chloride (157 mg, 0.215 mmol, 0.05 equiv), then sodium carbonate (4.83 mL, 1.0 M aqueous solution, 2.0 equiv). The reaction mixture heated in the microwave at 150° C. for 20 min. Purification by column chromatography using 2% methanol in dichloromethane elutions gave 1.04 g of the white solid, 60%.

Workup

customPurification by column chromatography

Sources & evidence

ORD record: ord-4d7d1459753a4ebdaf41b9256b890ce5
Source dataset: uspto-grants-2016_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09370515B2

Reaction notes

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